0363-0049 : Fexofenadine Hcl and Pseudoephedrine Hcl Oral Tablet, Extended Release


NDC: 0363-0049
Labeler: Walgreens Company
Product Type: Human OTC Drug
Drug Name:  Fexofenadine Hcl and Pseudoephedrine Hcl
Dosage Form: Oral Tablet, Extended Release
Application #: ANDA079043
Rev. Date: 


NDC Package Codes:

  • 0363-0049-10: 2 BLISTER PACK IN 1 CARTON (0363‑0049‑10) > 5 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK
  • 0363-0049-15: 3 BLISTER PACK IN 1 CARTON (0363‑0049‑15) > 5 TABLET, EXTENDED RELEASE IN 1 BLISTER PACK

Active Ingredients:

  • Fexofenadine Hydrochloride
  • Pseudoephedrine Hydrochloride

Dosage Strength:

  • 180 mg
  • 240 mg

Pharmaceutical Classes:

  • Adrenergic alpha-Agonists [MoA]
  • Histamine H1 Receptor Antagonists [MoA]
  • Histamine-1 Receptor Antagonist [EPC]
  • alpha-Adrenergic Agonist [EPC]

Related Products:

Based on records with the same trade name.
  • 0536-1394 Fexofenadine Hcl and Pseudoephedrine Hcl Oral Tablet, Extended Release by Rugby Laboratories
  • 43598-892 Fexofenadine Hcl and Pseudoephedrine Hcl Oral Tablet, Extended Release by Dr.reddy's Laboratories Inc
  • 51316-018 Fexofenadine Hcl and Pseudoephedrine Hcl Oral Tablet, Extended Release by Cvs Pharmacy, Inc
  • 55111-572 24 Hr Fexofenadine Hydrochloride 180 mg / Pseudoephedrine Hydrochloride 240 mg Extended Release Tablet by Dr.reddy's Laboratories Limited
  • 79903-255 Fexofenadine Hcl and Pseudoephedrine Hcl Oral Tablet, Extended Release by Walmart Inc.

NDC QR Code

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NDC 0363-0049 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.